Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development
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Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndromeMolecular basis of cleft palates in miceMultiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange SyndromeTooth agenesis and orofacial clefting: genetic brothers in arms?Prdm16 is required for normal palatogenesis in mice.Contrasting evolutionary dynamics of the developmental regulator PAX9, among bats, with evidence for a novel post-transcriptional regulatory mechanismSystematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts.The role of miR-31 and its target gene SATB2 in cancer-associated fibroblasts.Transferrin receptor facilitates TGF-β and BMP signaling activation to control craniofacial morphogenesis.Automated pipeline for anatomical phenotyping of mouse embryos using micro-CT.Molecular regulation of the developing commissural plateA network connecting Runx2, SATB2, and the miR-23a~27a~24-2 cluster regulates the osteoblast differentiation program.Unc5C and DCC act downstream of Ctip2 and Satb2 and contribute to corpus callosum formation.Molars and incisors: show your microarray IDs.Bmp and Shh signaling mediate the expression of satb2 in the pharyngeal arches.A cross-species analysis of Satb2 expression suggests deep conservation across vertebrate lineages.Critical-size calvarial bone defects healing in a mouse model with silk scaffolds and SATB2-modified iPSCsRoles of SATB2 in osteogenic differentiation and bone regenerationCharacterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontiaEnhanced osseointegration of titanium implant through the local delivery of transcription factor SATB2.Special AT-rich binding protein-2 (SATB2) differentially affects disease-causing p63 mutant proteins.Bmp signaling regulates a dose-dependent transcriptional program to control facial skeletal developmentGenetics of nonsyndromic orofacial cleftsThe mRNA expression of SATB1 and SATB2 in human breast cancer.Current knowledge of tooth development: patterning and mineralization of the murine dentition.SATB1 defines the developmental context for gene silencing by Xist in lymphoma and embryonic cells.X chromosome inactivation: a silence that needs to be broken.Developmental and genetic perspectives on Pierre Robin sequence.Left-right asymmetry of the gnathostome skull: its evolutionary, developmental, and functional aspects.Osteoblast-specific transcription factor Osterix (Osx) is an upstream regulator of Satb2 during bone formation.Special AT-rich sequence-binding protein 2 acts as a negative regulator of stemness in colorectal cancer cells.SATB2 suppresses gastric cancer cell proliferation and migration.Examination of a palatogenic gene program in zebrafish.Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.Implications of Vertebrate Craniodental Evo-Devo for Human Oral Health.SATB2 participates in regulation of menadione-induced apoptotic insults to osteoblasts.SATB2 gene variants in non-syndromic cleft lip with or without cleft palate in Indian population.Fgf8 dosage determines midfacial integration and polarity within the nasal and optic capsules.Effects of phenytoin on Satb2 and Hoxa2 gene expressions in mouse embryonic craniofacial tissue.Delineation of 2q32q35 deletion phenotypes: two apparent "proximal" and "distal" syndromes.
P2860
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P2860
Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development
description
2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2006
@ast
im Oktober 2006 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2006/10/01)
@sk
vědecký článek publikovaný v roce 2006
@cs
wetenschappelijk artikel (gepubliceerd op 2006/10/01)
@nl
наукова стаття, опублікована в жовтні 2006
@uk
مقالة علمية (نشرت في أكتوبر 2006)
@ar
name
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@ast
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@en
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@nl
type
label
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@ast
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@en
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@nl
prefLabel
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@ast
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@en
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@nl
P2093
P2860
P3181
P356
P1476
Satb2 haploinsufficiency pheno ...... oordination of jaw development
@en
P2093
Bethan L. Thomas
Isabelle Miletich
Manuela Schwark
Michael J. Depew
Olga Britanova
Victor Tarabykin
P2860
P304
P3181
P356
10.1086/508214
P407
P577
2006-10-01T00:00:00Z